Evidence map›Paper›PMID 41141881›Full record

ArticleCureus2025

Behind the Dizziness: A Clinical Journey to Wallenberg Syndrome.

Maaz Khalid, Madeena Mahmood

Abstract readCase Reports
In one paragraph

Article in Cureus, 2025. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Not yet cited in PubMed.

0numbers the graph read from it
0cells of the map it votes in
0citing papers in PubMed
–field-weighted citation impact
1 · What the graph read from it

What it found

Each row is one number read from the abstract, on the scale the paper reported it, with its interval. Left of the dashed line favours the treatment, right favours the comparator. Under each row is the sentence it came from. New to these charts? A ten-minute tutorial.

The abstract states no effect estimate the extractor could read, or names no intervention and outcome on the map, so this paper lights no cell and moves no belief. It is still indexed, cited and linked below.

2 · The registry

The trial behind it

Trials whose registry record cites this paper, or whose number appears in the abstract. A trial that started after this paper was published is citing it as background, not reporting it.

Neither the registry nor the abstract names a trial number. If this is a trial report, that itself is worth knowing.

3 · Its place in the literature

Who cites it

0 citing papers in PubMed.

No citing paper in PubMed yet.

4 · The record

Corrections and comments

PubMed lists nothing against this paper. Absence here is not a guarantee, only a check that was made.

5 · Who and what money

Authors and funding

2 authors.

Maaz KhalidInternal Medicine, The Royal Wolverhampton NHS Trust, Wolverhampton, GBR.
Madeena MahmoodGeneral Medicine, Mersey and West Lancashire Teaching Hospitals NHS Trust, Liverpool, GBR.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Wallenberg syndrome, also referred to as lateral medullary syndrome or posterior inferior cerebellar artery (PICA) syndrome, is a rare neurological disorder most often caused by occlusion of the PICA. It leads to infarction of the lateral medulla oblongata and presents with a range of symptoms, including vertigo, ataxia, cranial nerve deficits, and sensory disturbances. We present the case of a 41-year-old female who initially attended the emergency department (ED) with headache, nausea, and vomiting. She was treated for a urinary tract infection (UTI) with associated urinary retention. However, shortly after being discharged, she collapsed within the hospital grounds. Her medical history included hypertension and type 2 diabetes mellitus (T2DM). A computed tomography (CT) head scan showed no acute findings, but a subsequent magnetic resonance imaging (MRI) confirmed an acute left lateral medullary infarct, establishing the diagnosis of Wallenberg syndrome. This atypical presentation, which caused the misdiagnosis, can have a serious effect on the treatment of a stroke and the important decision to thrombolyse or not. This delay in treatment could cause long-term damage to the patient by affecting their day-to-day life.

Indexed as

acute ischaemic strokedual anti-platelet therapydw-mrihorner’s syndromelateral medullary syndrome (wallenberg syndrome)

Identifiers

PMID41141881
PMCPMC12552016

What OpenQuestion holds

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Registered trials

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Read under generation 80e0d062 · epoch 390. Bibliography from PubMed, PubMed Central and OpenAlex; grants from NIH RePORTER; trial links from ClinicalTrials.gov; estimates, votes and beliefs from the OpenQuestion graph.